Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,568 recalls have been distributed to Montana in the last 12 months.
Showing 3441–3460 of 48,326 recalls
Recalled Item: EOPA Arterial Cannula Recalled by Medtronic Perfusion Systems Due to...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Select Series Angled Tip Arterial Cannula Recalled by Medtronic Perfusion...
The Issue: Incorrect labeling for seven manufactured lots of certain models of Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROPONENT DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist Recalled by Abiomed, Inc. Due to Optical...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ESSENTIO DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VALITUDE CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCOLADE DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VISIONIST CRT-P Recalled by Boston Scientific Corporation Due to A subset of...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP with SmartAssist Recalled by Abiomed, Inc. Due to Optical Sensors...
The Issue: Optical Sensors have been damaged due to physical interaction between the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ALTRUA 2 DR Pacemaker Recalled by Boston Scientific Corporation Due to A...
The Issue: A subset of devices from the ACCOLADE Family of Pacemakers and CRT-Ps, built...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...
The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: chlorproMAZINE Hydrochloride Tablets Recalled by Glenmark Pharmaceuticals...
The Issue: CGMP Deviations: N-Nitroso-Desmethyl Chlorpromazine impurity (NNDCI) were...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Biological Recalled by HF Acquisition Co LLC Due to Spore test strip...
The Issue: Spore test strip monitoring system, designed for routine monitoring of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nuwellis AquaFlexFlow UF 500 Plus Recalled by Nuwellis Inc Due to The...
The Issue: The AquaFlexFlow UF 500 Plus extracorporeal blood circuit used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LITE Regener-Eyes Recalled by Regenerative Processing Plant, LLC Due to Lack...
The Issue: Lack of Sterility Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROFESSIONAL Regener-Eyes Recalled by Regenerative Processing Plant, LLC Due...
The Issue: Lack of Sterility Assurance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic NanoCross Elite PTA catheter Recalled by ev3 Inc Due to There is...
The Issue: There is the potential for in-vivo balloon deflation issues, including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Neo-Tee T-Piece Resuscitator Recalled by Mercury Enterprises, Inc. dba...
The Issue: Gas powered emergency resuscitator has a circuit flow controller...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.